- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01622244
Coordinated Access to Care From Hospital Emergency Departments (CATCH-ED)
October 29, 2014 updated by: Unity Health Toronto
Coordinated Access to Care From Hospital Emergency Departments - Assessing Effectiveness and Cost-Effectiveness
The study will assess the effectiveness and cost-effectiveness of providing brief, intensive case management for frequent users of hospital Emergency Departments who have mental health and/or addictions problems.
The goals of the intervention are to support patients' transition to community-based health and social services and supports - including primary and urgent psychiatric care, peer support and other community services and supports - so as to improve patient wellbeing and reduce avoidable ED visits and hospitalizations.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
166
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Toronto, Ontario, Canada, M5B 1W8
- St. Michael's Hospital
-
Toronto, Ontario, Canada, M5S 2N9
- St. Michael's Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- legal adult status (age 18)
- able to give informed consent
- have made 5+ visits to participating hospital Emergency Department in the previous 12 months
- One of these visits will have been for a mental health and/or addiction problem.
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention arm
Participants will receive brief, intensive case management to connect them to health and social services and supports in the community
|
brief, intensive case management for frequent users of hospital Emergency Departments who have mental health and/or addictions problems
Participants will receive brief, intensive case management to connect them to health and social services and supports in the community
|
Active Comparator: Counseling and Resource Education (CARE)
Participants will receive care as usual in the community.
In addition, participants in this arm will receive an educational session and resource guide outlining available community-based services
|
Participants will receive usual care as well as an educational session and resource guide outlining community-based services
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Frequency of Emergency Department visits
Time Frame: Baseline, 6 and 12 months
|
Baseline, 6 and 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes in symptom severity
Time Frame: Baseline, 6 and 12 months
|
A scales with good psychometric properties, the Colorado Symptom scale, will be used
|
Baseline, 6 and 12 months
|
Days in hospital
Time Frame: baseline, 6 and 12 months
|
baseline, 6 and 12 months
|
|
Changes in substance use
Time Frame: baseline 6 and 12 months
|
The Addiction Severity index will be used
|
baseline 6 and 12 months
|
Changes in health related quality of life
Time Frame: baseline, 6 and 12 months
|
The SF-12 and EQ-5D will be used
|
baseline, 6 and 12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Vicky Stergiopoulos, MD, MHSc, Unity Health Toronto
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2012
Primary Completion (Actual)
September 1, 2013
Study Completion (Actual)
September 1, 2014
Study Registration Dates
First Submitted
June 4, 2012
First Submitted That Met QC Criteria
June 14, 2012
First Posted (Estimate)
June 19, 2012
Study Record Updates
Last Update Posted (Estimate)
October 30, 2014
Last Update Submitted That Met QC Criteria
October 29, 2014
Last Verified
June 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- StMichael
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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